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NM_006086.3(TUBB3):c.292G>A (p.Gly98Ser) AND not provided

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Mar 18, 2016
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000255388.1

Allele description

NM_006086.3(TUBB3):c.292G>A (p.Gly98Ser)

Gene:
TUBB3:tubulin beta 3 class III [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q24.3
Genomic location:
Preferred name:
NM_006086.3(TUBB3):c.292G>A (p.Gly98Ser)
HGVS:
  • NC_000016.10:g.89934743G>A
  • NG_027810.1:g.17735G>A
  • NM_001197181.1:c.76G>A
  • NM_006086.3:c.292G>A
  • NP_001184110.1:p.Gly26Ser
  • NP_006077.2:p.Gly98Ser
  • NC_000016.9:g.90001151G>A
Protein change:
G26S
Links:
dbSNP: rs587784505
NCBI 1000 Genomes Browser:
rs587784505
Molecular consequence:
  • NM_001197181.1:c.76G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000321989GeneDx
criteria provided, single submitter

(GeneDx Variant Classification (06012015))		Pathogenic
(Mar 18, 2016) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV000321989.6

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The G98S variant in the TUBB3 gene has been reported previously as a de novo change in a child with congenital fibrosis of the extraocular muscles and structural abnormalities of the brain (Whitman et al., 2015). The G98S variant was not observed in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The G98S variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved across species. In silico analysis predicts this variant is probably damaging to the protein structure/function. We interpret G98S as a pathogenic variant.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Mar 31, 2019